Linked Data
ClinVar Variation Id:
38254
dbSNP Id:
rs397507432
gnomAD v2:
13-32971138-C-T
gnomAD v4:
13-32397001-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32397001C>T , CM000675.2:g.32397001C>T | GRCh38 |
| NC_000013.10:g.32971138C>T , CM000675.1:g.32971138C>T | GRCh37 |
| NC_000013.9:g.31869138C>T | NCBI36 |
| NG_012772.3:g.86522C>T , LRG_293:g.86522C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.*128C>T | ENSP00000434898.2:n.*128C>T | |
| ENST00000528762.2:c.*972C>T | ENSP00000433168.2:n.*972C>T | |
| ENST00000530893.7:c.9236C>T | ENSP00000499438.2:p.Pro3079Leu | |
| ENST00000665585.2:c.*1167C>T | ENSP00000499570.2:n.*1167C>T | |
| ENST00000700202.2:c.9554C>T | ENSP00000514856.2:p.Pro3185Leu | |
| ENST00000700202.1:c.2021C>T | ENSP00000514856.1:p.Pro674Leu | |
| ENST00000700203.1:n.1732C>T | ||
| ENST00000380152.8:c.9605C>T MANE Select | ENSP00000369497.3:p.Pro3202Leu | |
| ENST00000544455.6:c.9605C>T | ENSP00000439902.1:p.Pro3202Leu | |
| ENST00000614259.2:c.9613C>T | ENSP00000506251.1:n.9613C>T | |
| ENST00000665585.1:c.2483C>T | ||
| ENST00000680887.1:c.9605C>T | ENSP00000505508.1:p.Pro3202Leu | |
| ENST00000380152.7:c.9605C>T | ENSP00000369497.3:p.Pro3202Leu | |
| ENST00000470094.1:c.688C>T | ||
| ENST00000533776.1:n.193C>T | ||
| ENST00000544455.5:c.9605C>T | ENSP00000439902.1:p.Pro3202Leu | |
| NM_000059.3:c.9605C>T , LRG_293t1:c.9605C>T | NP_000050.2:p.Pro3202Leu | |
| XM_011535203.1:c.9605C>T | XP_011533505.1:p.Pro3202Leu | |
| XM_011535204.1:c.9509C>T | XP_011533506.1:p.Pro3170Leu | |
| NM_000059.4:c.9605C>T MANE Select | NP_000050.3:p.Pro3202Leu |